Results 91 to 100 of about 5,149 (199)
Fibroblast growth factor signaling in skeletal development and disease [PDF]
, 2015 Fibroblast growth factor (FGF) signaling pathways are essential regulators of vertebrate skeletal development. FGF signaling regulates development of the limb bud and formation of the mesenchymal condensation and has key roles in regulating ...
Marie, Pierre J, Ornitz, David M
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Apert Syndrome: orthopedic treatment [PDF]
, 2011 El Síndrome de Apert es un trastorno autosómico dominante, caracterizado por craneosinostosis, hipoplasia del tercio medio de la cara y sindactilia de manos y pies.
Alonso Tajes, Francisco +3 more
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Premature Craniosynostosis in a Rare Genetic Disease- A Case Report
Iranian Journal of Public Health, 2015 Background: Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity.Its most notable characteristic feature is premature synostosis of cranial sutures .The case presented is ...
Hasnain Abbas Dharamshi +6 more
doaj
Disease Models & Mechanisms, 2018 FGFR2c regulates many aspects of craniofacial and skeletal development. Mutations in the FGFR2 gene are causative of multiple forms of syndromic craniosynostosis, including Crouzon syndrome.
Kevin K. L. Lee +7 more
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An exploration of the cognitive, physical and psychosocial development of children with Apert syndrome [PDF]
, 2016 Apert syndrome is a rare condition, with a birth prevalence of approximately 1 in 65 000. This article provides an up to date review of the literature on Apert syndrome from a variety of perspectives, ranging from surgical management to personal accounts.
Hilton, C
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Oral manifestations of Crouzon Syndrome and their implications for dental care: case report [PDF]
RGO: Revista Gaúcha de OdontologiaCrouzon Syndrome is a rare genetic disease that affects craniofacial development resulting in various manifestations in the head and neck region. This article aimed to report a clinical case of a patient with Crouzon Syndrome, highlighting the relevant ...
Ana Paula Otoni Sena +5 more
doaj +1 more source
Development, Disease, and Regeneration of Tissues in the Dental-Craniofacial Complex [PDF]
, 2013 This article has no ...
Chun, Yong-Hee P. +5 more
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Crouzon syndrome: Genetic and intervention review
Journal of Oral Biology and Craniofacial Research, 2019 Crouzon syndrome exhibits considerable phenotypic heterogeneity, in the aetiology of which genetics play an important role. FGFR2 mediates extracellular signals into cells and the mutations in the FGFR2 gene cause this syndrome occurrence. Activated FGFs/
N.M. Al-Namnam +3 more
doaj +1 more source
Prevalence and treatment outcomes of hydrocephalus among children with craniofacial syndromes
Journal of Plastic Surgery and Hand SurgeryIntroduction: Hydrocephalus is more common in patients with craniofacial syndromes (CS) relative to non-syndromic craniosynostosis, and the optimal management is challenging.
Saga Jönsson +6 more
doaj +1 more source
Crouzon\'s Syndrome: A Case Report
International Journal of Clinical Pediatric Dentistry, 2013 Crouzon's syndrome (CS) is a rare autosomal dominant condition with multiple mutations of the fibroblast growth factor receptor (FGFR2) gene, which accounts for 4.8% of all cases of craniosynostosis. It is characterized by premature closure of cranial sutures, cranial deformities, midface hypoplasia, relative mandibular prognathism, hypertelorism ...
Kumar, G Ravi +3 more
openaire +2 more sources